For researchers

Is your paper here?

2,677 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

62 matches for Porteous D, showing the first 20.

New gene functions in megakaryopoiesis and platelet formation
Nature · 2011 · PMID 22139419
12 pages+
rs3811444 rs625132 rs17030845 rs7616006 rs1354034 rs399604
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs12142680 rs56044892 rs12410444 rs12754946 rs1008078 rs17372140
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
International Consortium of Blood Pressure (ICBP) 1000G Analyses · BIOS Consortium and 9 more consortia
Nature genetics · 2017 · PMID 28135244 · open access
12 pages+
rs1566497 rs6081613 rs8258 rs117006983 rs9323988 rs4952611
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
rs7872188 rs10870202 rs10515750 rs113745635 rs11658500 rs1458979
Genetic prediction of male pattern baldness
PLoS genetics · 2017 · PMID 28196072 · open access
12 pages+
rs79284724 rs17752365 rs1842202 rs73209413 rs113222435 rs73212804
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
rs755546258 rs72742734 rs554379257 rs184469050 rs7952436 rs139770682
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
rs60848348 rs1454934 rs36004974 rs577676 rs11598047 rs10800507
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
rs6012558 rs4239436 rs6772896 rs765751 rs2645294 rs12679556
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
rs7175517 rs1406948 rs10923724 rs2371767 rs7766106 rs10101061
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs71324996 rs8070135 rs151231 rs954734 rs62170823 rs926300
Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs34216058 rs56322472 rs67630759 rs75278839 rs2165934 rs34654885
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
rs12967143 rs198457 rs7117514 rs57344483 rs3213572 rs1343605
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs2236180 rs10836366 rs1985511 rs11205354 rs1215 rs34093919
Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life
Molecular psychiatry · 2020 · PMID 30867560 · open access
12 pages+
rs35031964 rs80035064 rs1109618 rs11985603 rs4841335 rs7841921
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs679843 rs10964603 rs924981 rs35636653 rs1078442 rs4918943
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs7315236 rs699465 rs10414501 rs77951490 rs78863347 rs9271585

Showing 20 of 62 · page 1 of 4

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.